Glukhovsky A, Adam D R, Amitzur G, Sideman S
Department of Biomedical Engineering, Heart System Research Center, The Julius Silver Institute, Technion-Israel Institute of Technology, Haifa, Israel.
Ann Biomed Eng. 1998 Mar-Apr;26(2):213-29. doi: 10.1114/1.54.
The proposed model describes myocyte calcium (Ca++) cycling, emphasizing the kinetics of sarcoplasmic reticulum (SR) Ca++ release channels. The suggested SR channel regulating mechanism includes two types of Ca++ binding sites: (1) low affinity sites with high binding rates, regulating the opening of Ca++ channels and (2) high affinity sites with low binding rates, which regulate their closing. The amount of Ca++ released from the SR and the peak value of Ca++ ion concentration [Ca++] in the cytoplasm were found to depend on the rate of the increase of [Ca++], similar to Ca++ induced Ca++ release experiments. The model describes spontaneous release of Ca++ from overloaded SR. The dependence of the control mechanism on the activating and inactivating sites is substantiated by simulations of ryanodine intervention, providing results similar to experimental results. Simulations under conditions of isolated SR vesicles produced Ca++ release results similar to measured data. Consequently, it is suggested that the recovery of Ca++ release channels represents the rate limiting factor in the process of mechanical restitution.
所提出的模型描述了心肌细胞钙(Ca++)循环,着重强调了肌浆网(SR)钙释放通道的动力学。所建议的SR通道调节机制包括两种类型的Ca++结合位点:(1)具有高结合速率的低亲和力位点,调节Ca++通道的开放;(2)具有低结合速率的高亲和力位点,调节其关闭。发现从SR释放的Ca++量和细胞质中Ca++离子浓度[Ca++]的峰值取决于[Ca++]的增加速率,这与Ca++诱导的Ca++释放实验类似。该模型描述了过载SR中Ca++的自发释放。通过对雷诺丁干预的模拟证实了控制机制对激活和失活位点的依赖性,提供了与实验结果相似的结果。在分离的SR囊泡条件下的模拟产生了与测量数据相似的Ca++释放结果。因此,有人提出Ca++释放通道的恢复是机械恢复过程中的速率限制因素。